Insulin Lispro (Humalog) injectable bulk supplier for pharma manufacturers

Insulin Lispro (Humalog) Injectable Suppliers & Bulk Manufacturers

Available Forms: Vials/pens

Available Strengths: U-100, U-200

Reference Brands: Humalog, Admelog, Fiasp(US); Humalog, Fiasp(EU)

Category: Diabetes

Insulin Lispro (Humalog) injectable is available in Vials/pens and strengths such as U-100, U-200. Sourced from GMP-certified and ISO-compliant manufacturers, this API meets global pharmacopeia standards (USP/EP/JP as applicable). Ideal for pharmaceutical formulation and commercial manufacturing, Insulin Lispro (Humalog) injectable is supplied in bulk quantities with complete regulatory support including DMF, COA, and MSDS.

Technical Specifications & Supply Details
Lead Time 7 to 60 days (depending on batch size & schedule)
MOQ As per manufacturer’s batch size
COA Available with every batch
Regulatory Dossier / DMF Available upon request
Export Documentation FSC, COA, Manufacturing License, Product Permission
Standards IP, BP, USP
Certifications WHO-GMP, EU-GMP, USFDA (as applicable)

Insulin Lispro (Humalog) injectable can be exported to over 30 countries across Asia, Africa, Europe, and Latin America. Flexible packaging, competitive pricing, and a verified supplier network make Pharmatradz a trusted sourcing partner for pharmaceutical companies and contract manufacturers worldwide.

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📘 Sourcing Guide

Product Description:

Insulin Lispro (Humalog) is a rapid-acting insulin approved in the EU and US for post-meal blood glucose control. In the EU, Novo Nordisk’s Fiasp, a faster-acting version, is regulated by EMA with dossiers demonstrating safety, efficacy, and manufacturing quality. In the US, the FDA has approved Humalog and biosimilars like Admelog based on comprehensive clinical data, biosimilarity, and ongoing pharmacovigilance. Both regions require detailed regulatory dossiers for approval and post-marketing safety monitoring. For expert assistance with pharmaceutical dossiers and compliance, visit PharmaTradz, your trusted partner in regulatory solutions.

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Frequently Asked Questions

What is Insulin Lispro made from? Insulin Lispro is a recombinant human insulin analogue produced using recombinant DNA technology in Escherichia coli bacteria. It differs from human insulin by the reversal of two amino acids—proline and lysine—at positions 28 and 29 on the B-chain, which allows it to act faster in the body.

What is Insulin Lispro trade name? The trade name for Insulin Lispro is Humalog.

What company makes Insulin Lispro? Insulin Lispro (Humalog) is manufactured by Eli Lilly and Company.

What is generic name of Insulin Lispro? The generic name of this product is Insulin Lispro.

What is brand name of Insulin Lispro? The brand name of Insulin Lispro is Humalog.

Where is Insulin Lispro manufactured? Insulin Lispro is manufactured by Eli Lilly and Company, with production facilities located in the United States and several other countries, including France and Italy, depending on the regional supply chain.

Yes, Insulin Lispro (Humalog) injectable is available with DMF and other regulatory documents such as COA and MSDS. These can be provided upon request for qualified buyers.

Absolutely. Sample requests are accepted for formulation trials and quality checks. Please submit an enquiry to initiate the process.

Our manufacturing partners are GMP-certified and comply with ISO and WHO standards, ensuring global quality benchmarks.

Lead times vary based on quantity and destination, but most orders are fulfilled within 1–3 weeks. Express shipping options are available.

Yes, Insulin Lispro (Humalog) injectable is exported to over 30 countries across Asia, Africa, Europe, and Latin America. We support documentation for customs and regulatory clearance.

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